Variant #0001053233 (NC_000009.11:g.34647855C>T, NM_001142784.2:c.-4376C>T (IL11RA))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.34647855C>T
DNA change (hg38) -
Published as GALT(NM_000155.3):c.404C>T (p.S135L), GALT(NM_000155.4):c.404C>T (p.(Ser135Leu))
ISCN -
DB-ID GALT_000005 See all 4 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00025 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GALT NM_000155.3 +/. - c.404C>T r.(?) p.(Ser135Leu)
IL11RA NM_001142784.2 +/. - c.-4376C>T r.(?) p.(=)
CCL27 NM_006664.2 +/. - c.*14086G>A r.(=) p.(=)


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